Department of Neurological Sciences, Rush University Medical Center, Chicago, Illinois 60612, USA.
J Biol Chem. 2013 Jun 21;288(25):18533-45. doi: 10.1074/jbc.M112.447268. Epub 2013 May 7.
Ciliary neurotrophic factor (CNTF) is a promyelinating trophic factor, and the mechanisms by which CNTF expression could be increased in the brain are poorly understood. Acetylsalicylic acid (aspirin) is one of the most widely used analgesics. Interestingly, aspirin increased mRNA and protein expression of CNTF in primary mouse and human astrocytes in a dose- and time-dependent manner. Aspirin induced the activation of protein kinase A (PKA) but not protein kinase C (PKC). H-89, an inhibitor of PKA, abrogated aspirin-induced expression of CNTF. The activation of cAMP-response element-binding protein (CREB), but not NF-κB, by aspirin, the abrogation of aspirin-induced expression of CNTF by siRNA knockdown of CREB, the presence of a consensus cAMP-response element in the promoter of CNTF, and the recruitment of CREB and CREB-binding protein to the CNTF promoter by aspirin suggest that aspirin increases the expression of the Cntf gene via the activation of CREB. Furthermore, we demonstrate that aspirin-induced astroglial CNTF was also functionally active and that supernatants of aspirin-treated astrocytes of wild type, but not Cntf null, mice increased myelin-associated proteins in oligodendrocytes and protected oligodendrocytes from TNF-α insult. These results highlight a new and novel myelinogenic property of aspirin, which may be of benefit for multiple sclerosis and other demyelinating disorders.
睫状神经营养因子(CNTF)是一种促髓鞘形成的营养因子,但大脑中 CNTF 表达增加的机制尚不清楚。乙酰水杨酸(阿司匹林)是最广泛使用的镇痛药之一。有趣的是,阿司匹林以剂量和时间依赖的方式增加原代小鼠和人星形胶质细胞中 CNTF 的 mRNA 和蛋白表达。阿司匹林诱导蛋白激酶 A(PKA)的激活,但不诱导蛋白激酶 C(PKC)的激活。PKA 的抑制剂 H-89 阻断了阿司匹林诱导的 CNTF 表达。阿司匹林激活 cAMP 反应元件结合蛋白(CREB),而不是 NF-κB,siRNA 敲低 CREB 可阻断阿司匹林诱导的 CNTF 表达,CNTF 启动子中存在一个公认的 cAMP 反应元件,以及阿司匹林募集 CREB 和 CREB 结合蛋白到 CNTF 启动子,提示阿司匹林通过激活 CREB 增加 Cntf 基因的表达。此外,我们证明阿司匹林诱导的星形胶质细胞 CNTF 也具有功能活性,并且野生型阿司匹林处理的星形胶质细胞上清液可增加少突胶质细胞中的髓鞘相关蛋白,并可防止 TNF-α 对少突胶质细胞的损伤。这些结果突出了阿司匹林的一种新的髓鞘形成特性,这可能对多发性硬化症和其他脱髓鞘疾病有益。